Chatzifrangkeskou Maria, Perdiou Alexandra, Kreouzou Revekka, Zissimou Georgia A, Flesariu Dragos F, Koutentis Panayiotis A, Skourides Paris A
Department of Biological Sciences, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus.
Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus.
Cells. 2025 May 9;14(10):688. doi: 10.3390/cells14100688.
Motile cilia play essential roles in various physiological processes including fluid flow generation and sperm motility. In this study, we identified 1,3-diphenyl-6-(4-phenylpiperazin-1-yl)benzo[][1,2,4]triazin-7(1)-one as a potent and reversible modulator of ciliary function using the model. This benzotriazinone derivative inhibits ciliary-driven fluid flow by inducing cilia detachment without causing toxicity in developing embryos. Unlike traditional deciliation agents that rely on calcium signaling, this compound induces cilia loss through a shear stress-driven mechanism at the transition zone, without disrupting tissue morphology or the apical actin network. Importantly, it also induces flagellar loss and impairs sperm motility at picomolar concentrations. Our findings highlight the potential of this 6-(4-phenylpiperazin-1-yl)-substituted benzotriazinone as a non-hormonal male contraceptive and underscore a novel mechanism of cilia modulation that may have broader implications for the treatment of cilia-related disorders.
运动性纤毛在包括流体流动产生和精子运动在内的各种生理过程中发挥着重要作用。在本研究中,我们使用该模型鉴定出1,3 - 二苯基 - 6 -(4 - 苯基哌嗪 - 1 - 基)苯并[][1,2,4]三嗪 - 7(1) - 酮是一种有效的、可逆的纤毛功能调节剂。这种苯并三嗪酮衍生物通过诱导纤毛脱离来抑制纤毛驱动的流体流动,而不会对发育中的胚胎产生毒性。与依赖钙信号传导的传统去纤毛剂不同,该化合物通过在过渡区由剪切应力驱动的机制诱导纤毛丧失,而不会破坏组织形态或顶端肌动蛋白网络。重要的是,它在皮摩尔浓度下还会诱导鞭毛丧失并损害精子运动。我们的研究结果突出了这种6 -(4 - 苯基哌嗪 - 1 - 基)取代的苯并三嗪酮作为非激素男性避孕药的潜力,并强调了一种新的纤毛调节机制,这可能对纤毛相关疾病的治疗具有更广泛的意义。